Genomic variant #0000736230

Individual ID 00000003
Chromosome 19
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.1044754T>C
Reference dbSNP
DB-ID ABCA7_000092
Frequency 0.714
Allele Count 150
Allele Number 210
Depth 890
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA7 NM_019112.3 ./.
ABCA7 XM_006722616.1 ./.
ABCA7 XM_006722617.2 ./.
ABCA7 XM_006722618.2 ./.
ABCA7 XM_011527628.1 ./.
ABCA7 XM_011527629.1 ./.
ABCA7 XM_011527630.1 ./.
ABCA7 XM_011527631.1 ./.
ABCA7 XM_011527632.1 ./.
ABCA7 XM_011527633.1 ./.
ABCA7 XM_011527634.1 ./.
ABCA7 XM_011527635.1 ./.
ABCA7 XM_011527636.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin